That's a lot of food for thought.
I agree we're probably going to have to be thinking of something like the annual flu vaccine. I don't know how willing people will be to take it up. The take up, I think, of flu jabs amongst older people has been quite good in the past, although I've never looked at the figures, so that is just my perception. But there's been so much relentless anti-vax stuff that I think there's a very widespread resistance to vaccination even amongst people who, a couple of years ago, wouldn't have thought twice about having one.
I take on board what you say about bedridden, but if those are people that previously would have been on ventilators, then that to me still seems like an improvement if one's thinking in terms of survival.
On the other hand, is what such people are going through getting the attention it needs in terms of awareness and support? As I type this, I'm not convinced it is.
That being said, something that's bugged me throughout this relates to long covid. It became apparent quite early in the pandemic and groups of people with it were getting together to exchange information, research it, then liaise with people with other sorts of conditions involving long-term fatigue and/or post-viral conditions. That seemed to be progressing then went relatively quiet.
I'm afraid I'm cynical enough (and I hope I'm wrong) to think that except for a bit of aftercare for the most ill, a lot will find themselves in the same position as those with a range of other conditions, most notably ME/CFS, that are often put down to 'all in the mind' or even 'faking it'. This is an important thing to do in any context where they can be expensive and, I believe, originates in America in terms of healthcare, and also has roots in a variety of countries, including ours, that have done the sort of things our governments have with sickness/disability benefits, e.g. Australia, Canada etc.
Tell people they're faking it, imagining it, exaggerating it and you can refuse to spend money on them
So I then turn back to 'very nasty flu at home' version of the virus. Will that be adequately acknowledged and supported?
It doesn't help that it's known that there's a nastier version of the common cold going round, and also flu's back with the possibility of new mutations and under-vaccination. How are people supposed to know which they've got, and if they do, get the right help?
Then add in all the nastiness of the benefits system which encourages people to 'man up' and go to work if they have a job and hey presto, more spreading.
Picking up on this
It worries me personally. Not that I think I would die or need hospital if I caught it but I don't have a support network, live alone and know no one to help with the dog and have no idea how I would manage if I was very ill at home.
I have a bit of a support network, but not much of one. I worry about things even as simple as whether, if I was in hospital, I'd be able to contact a neighbour to go round and sort out the heating etc., and to sort out anti-burglar stuff like making sure my light timers were on and my radio batteries replenished. (I reckon my radio's a bigger burglar deterrent than my alarm.)
Having had postviral fatigue accepted and recognised twice and then later had it again and had it dismissed as 'retarded depression', I see the difference it makes what labels people stick on you.
I'm lucky in one respect - where I live, there's a community network you can ask for help. It also gets extended informally. But I don't know how much I could rely on it or for how long.
I wonder whether those of us with chronic disabilities have a greater awareness than many (but far from all) others of the difficulties of dealing with debilitating conditions with inadequate support, which, added to our potentially increased vulnerability (depending on our underlying conditions) makes the thought of things like this very anxiety-inducing.
I hope this doesn't come out wrong, but whilst I wish you didn't feel the way you do, knowing you feel that way reminds me I'm not alone with some of my worries about it, which helps me a little.